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维生素D受体Fok1和Bsm 1基因多态性与系统性红斑狼疮和骨关节炎:自身免疫性炎症与退行性模型

Vitamin D receptor Fok1 & Bsm 1 Gene Polymorphisms in Systemic Lupus Erythematosus and Osteoarthritis: Autoimmune Inflammatory versus Degenerative Model.

作者信息

Ghaly Mona S, Badra Dahlia I, Dessouki Omar, Elmaraghy Nermine N, Hassan Ranya

机构信息

Department of Rheumatology & Rehabilitation, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.

Department of Medical Biochemistry, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.

出版信息

Egypt J Immunol. 2017 Jun;24(2):151-164.

Abstract

Vitamin D deficiency has been described in SLE and OA. Low vitamin D level is prevalent in Egyptian SLE patients while controversial studies are present regarding its level in OA patients in Egypt. We investigated whether vitamin D receptor (VDR) genes Bsm1 and Fok1 polymorphisms could be used as genetic markers for the susceptibility to SLE and /or OA in a sample of Egyptian population. The study was carried out on 100 SLE patients, 100 osteoarthritic patients and 100 normal controls using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP). Our results showed a statistically significant difference in Fok1 genotype distribution between SLE and OA patients (p=0.001). In SLE group, the "f" allele was significantly over-represented where 30% had "f" allele compared to 0% in OA (P = 0.03). Fok1 ff genotypes showed a significant association with disease activity in SLE patients. In addition, the fb haplotype frequency was significantly higher in SLE patients than controls (P=0.01). In conclusion Fok1 genotype and f allelic frequencies may be susceptible risk factors for SLE rather than OA in Egyptian patients.

摘要

维生素D缺乏在系统性红斑狼疮(SLE)和骨关节炎(OA)中已有报道。埃及SLE患者中维生素D水平较低,而关于埃及OA患者维生素D水平的研究存在争议。我们调查了维生素D受体(VDR)基因Bsm1和Fok1多态性是否可作为埃及人群样本中SLE和/或OA易感性的遗传标记。本研究采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术,对100例SLE患者、100例骨关节炎患者和100例正常对照进行了研究。我们的结果显示,SLE患者和OA患者之间Fok1基因型分布存在统计学显著差异(p = 0.001)。在SLE组中,“f”等位基因明显占优势,30%的患者有“f”等位基因,而OA患者中这一比例为0%(P = 0.03)。Fok1 ff基因型与SLE患者的疾病活动显著相关。此外,SLE患者的fb单倍型频率显著高于对照组(P = 0.01)。总之,在埃及患者中,Fok1基因型和f等位基因频率可能是SLE而非OA的易感风险因素。

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